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Genetics Modulate Gray Matter Variation Beyond Disease Burden in Prodromal Huntington’s Disease

Overview of attention for article published in Frontiers in Neurology, March 2018
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  • In the top 25% of all research outputs scored by Altmetric
  • Good Attention Score compared to outputs of the same age (74th percentile)
  • Good Attention Score compared to outputs of the same age and source (78th percentile)

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Title
Genetics Modulate Gray Matter Variation Beyond Disease Burden in Prodromal Huntington’s Disease
Published in
Frontiers in Neurology, March 2018
DOI 10.3389/fneur.2018.00190
Pubmed ID
Authors

Jingyu Liu, Jennifer Ciarochi, Vince D. Calhoun, Jane S. Paulsen, H. Jeremy Bockholt, Hans J. Johnson, Jeffrey D. Long, Dongdong Lin, Flor A. Espinoza, Maria B. Misiura, Arvind Caprihan, Jessica A. Turner, PREDICT-HD Investigators and Coordinators of the Huntington Study Group

Abstract

Huntington's disease (HD) is a neurodegenerative disorder caused by an expansion mutation of the cytosine-adenine-guanine (CAG) trinucleotide in the HTT gene. Decline in cognitive and motor functioning during the prodromal phase has been reported, and understanding genetic influences on prodromal disease progression beyond CAG will benefit intervention therapies. From a prodromal HD cohort (N = 715), we extracted gray matter (GM) components through independent component analysis and tested them for associations with cognitive and motor functioning that cannot be accounted for by CAG-induced disease burden (cumulative effects of CAG expansion and age). Furthermore, we examined genetic associations (at the genomic, HD pathway, and candidate region levels) with the GM components that were related to functional decline. After accounting for disease burden, GM in a component containing cuneus, lingual, and middle occipital regions was positively associated with attention and working memory performance, and the effect size was about a tenth of that of disease burden. Prodromal participants with at least one dystonia sign also had significantly lower GM volume in a bilateral inferior parietal component than participants without dystonia, after controlling for the disease burden. Two single-nucleotide polymorphisms (SNPs: rs71358386 in NCOR1 and rs71358386 in ADORA2B) in the HD pathway were significantly associated with GM volume in the cuneus component, with minor alleles being linked to reduced GM volume. Additionally, homozygous minor allele carriers of SNPs in a candidate region of ch15q13.3 had significantly higher GM volume in the inferior parietal component, and one minor allele copy was associated with a total motor score decrease of 0.14 U. Our findings depict an early genetical GM reduction in prodromal HD that occurs irrespective of disease burden and affects regions important for cognitive and motor functioning.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 27 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 27 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 6 22%
Student > Master 3 11%
Other 2 7%
Professor > Associate Professor 2 7%
Student > Ph. D. Student 2 7%
Other 3 11%
Unknown 9 33%
Readers by discipline Count As %
Medicine and Dentistry 5 19%
Psychology 3 11%
Neuroscience 3 11%
Nursing and Health Professions 1 4%
Economics, Econometrics and Finance 1 4%
Other 4 15%
Unknown 10 37%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 8. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 12 April 2018.
All research outputs
#4,152,445
of 23,031,582 outputs
Outputs from Frontiers in Neurology
#3,416
of 11,923 outputs
Outputs of similar age
#82,466
of 329,870 outputs
Outputs of similar age from Frontiers in Neurology
#56
of 263 outputs
Altmetric has tracked 23,031,582 research outputs across all sources so far. Compared to these this one has done well and is in the 81st percentile: it's in the top 25% of all research outputs ever tracked by Altmetric.
So far Altmetric has tracked 11,923 research outputs from this source. They typically receive a little more attention than average, with a mean Attention Score of 7.3. This one has gotten more attention than average, scoring higher than 71% of its peers.
Older research outputs will score higher simply because they've had more time to accumulate mentions. To account for age we can compare this Altmetric Attention Score to the 329,870 tracked outputs that were published within six weeks on either side of this one in any source. This one has gotten more attention than average, scoring higher than 74% of its contemporaries.
We're also able to compare this research output to 263 others from the same source and published within six weeks on either side of this one. This one has done well, scoring higher than 78% of its contemporaries.